| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6963102-6963240 | Rare:28 | ||||
| chr12:7970713-7970988 | Rare:80 | ||||
| chr12:8242940-8243219 | Common:8; Rare:82 | ||||
| chr12:8285810-8285992 | Common:1; Rare:39 | ||||
| chr12:9093468-9093805 | Common:3; Rare:81; Clinvar (benign):1 | ||||
| chr12:9107527-9107829 | Common:4; Rare:58 | ||||
| chr12:9112508-9112675 | Rare:38 | ||||
| chr12:9240324-9240400 | Common:1; Rare:15 | ||||
| chr12:9448170-9448328 | Common:1; Rare:76 | ||||
| chr12:12808071-12808207 | Common:1; Rare:17 | ||||
| chr12:24562096-24562143 | Common:2; Rare:9 | ||||
| chr12:24562361-24562430 | Rare:13 | ||||
| chr12:24562436-24562521 | Common:1; Rare:31 | ||||
| chr12:42465098-42465444 | Rare:68; Clinvar:3; Clinvar (benign):5 | ||||
| chr12:45727482-45727597 | Rare:59 |